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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799043Generated: October 30, 2026

Hydrochloric Acid → 3-hydroxy-2-hydroxymethyl-2-[4-(9-hydroxy-2-methyl-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-propionic acid

https://huagongshe.com/reaction/1799043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDimethylformamideHCID 6228—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactantt-butyl[4-(9-hydroxy-2-methyl-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-acetateHCID 59492691—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-hydroxy-2-hydroxymethyl-2-[4-(9-hydroxy-2-methyl-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-propionic acidHCID 59492687—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of an optically active form (17.8 g) of t-butyl[4-(9-hydroxy-2-methyl-9-trifluoromethyl-9H-fluoren-4-yl)-pyrazol-1-yl]-acetate and paraformaldehyde (12.0 g) in dimethylformamide (60 ml) was added at room temperature a 1M solution (120 ml) of tetrabutylammonium fluoride in tetrahydrofuran, and the mixture was stirred at 95° C. for 3 hr. To the reaction mixture were added 1N hydrochloric acid (180 ml) and water (90 ml), and the mixture was extracted with ethyl acetate (180 ml). The separated aqueous layer was extracted twice with ethyl acetate (90 ml). The combined organic layer was successively washed once with 1N hydrochloric acid (90 ml), twice with water (90 ml) and once with saturated brine (90 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the title compound (15.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343994B2
Source datasetuspto-grants-2013_01
ORD IDord-c7efb0ec634941c5b2d6d809a9cb2ba7
Source noteuspto-grants-2013_01